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  1. 1
    Calcinosis cutis in autoimmune connective tissue diseases

    Calcinosis cutis in autoimmune connective tissue diseases by Albert Gutierrez, David A. Wetter

    Published 2012
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  2. 2
    Marfan's syndrome: an overview

    Marfan's syndrome: an overview by Shi‐Min Yuan, Hua Jing

    Published 2010
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  3. 3
    Large aortic aneurysm and dissection in a patient with Marfan s syndrome

    Large aortic aneurysm and dissection in a patient with Marfan s syndrome by Fernando Pivatto Júnior, Leila Denise Cardoso Ramos, Murilo Foppa, Felipe Soares Torres

    Published 2015
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  4. 4
    Mechanisms in the loss of capillaries in systemic sclerosis: angiogenesis <i>versus</i> vasculogenesis

    Mechanisms in the loss of capillaries in systemic sclerosis: angiogenesis <i>versus</i> vasculogenesis by Mirko Manetti, Serena Guiducci, Lidia Ibba‐Manneschi, Marco Matucci‐Cerinic

    Published 2010
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  5. 5
    Ehlers-Danlos Syndrome, Hypermobility Type: An Underdiagnosed Hereditary Connective Tissue Disorder with Mucocutaneous, Articular, and Systemic Manifestations

    Ehlers-Danlos Syndrome, Hypermobility Type: An Underdiagnosed Hereditary Connective Tissue Disorder with Mucocutaneous, Articular, and Systemic Manifestations by Marco Castori

    Published 2012
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  6. 6
    Recent progress in genetics of Marfan syndrome and Marfan-associated disorders

    Recent progress in genetics of Marfan syndrome and Marfan-associated disorders by Takeshi Mizuguchi, Naomichi Matsumoto

    Published 2006
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  7. 7
    Mutations in <i>FKBP10</i> cause recessive osteogenesis imperfecta and bruck syndrome

    Mutations in <i>FKBP10</i> cause recessive osteogenesis imperfecta and bruck syndrome by Brian Kelley, Fransiska Malfait, Luisa Bonafé, Dustin Baldridge, Erica P. Homan, Sofie Symoens, Andy Willaert, Nursel Elçioğlu, Lionel Van Maldergem, Christine Verellen‐Dumoulin, Y. Gillerot, Dobrawa Napierala, Deborah Krakow, Peter Beighton, Andrea Superti‐Furga, Anne De Paepe, Brendan Lee

    Published 2010
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  8. 8
    Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies

    Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies by Caroline Hayward, D. J. H. Brock

    Published 1997
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  9. 9
    Ectopic mineralization disorders of the extracellular matrix of connective tissue: Molecular genetics and pathomechanisms of aberrant calcification

    Ectopic mineralization disorders of the extracellular matrix of connective tissue: Molecular genetics and pathomechanisms of aberrant calcification by Qiaoli Li, Qiujie Jiang, Jouni Uitto

    Published 2013
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  10. 10
    Cystic medial necrosis: pathological findings and clinical implications

    Cystic medial necrosis: pathological findings and clinical implications by Shi‐Min Yuan, Jing Hua

    Published 2011
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  11. 11
    Neurovascular manifestations of heritable connective tissue disorders. A review.

    Neurovascular manifestations of heritable connective tissue disorders. A review. by Wouter I. Schievink, Virginia V. Michels, D. G. Piepgras

    Published 1994
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  12. 12
    Otolaryngological Aspects of Sjogren's Syndrome

    Otolaryngological Aspects of Sjogren's Syndrome by J. A. Doig, K Whaley, W. Carson Dick, G. Nuki, John Williamson, W. Watson Buchanan

    Published 1971
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  13. 13
    Coronary artery aneurysms in patients with hyper IgE recurrent infection syndrome

    Coronary artery aneurysms in patients with hyper IgE recurrent infection syndrome by Jennifer C. Ling, Alexandra F. Freeman, Ahmed M. Gharib, Andrew E. Arai, Robert J. Lederman, Douglas R. Rosing, Steven M. Holland

    Published 2006
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  14. 14
    Transgenic mouse model of the mild dominant form of osteogenesis imperfecta.

    Transgenic mouse model of the mild dominant form of osteogenesis imperfecta. by J Bonadio, Thomas L. Saunders, Emily J. Tsai, Steven A. Goldstein, J. Morris-Wiman, L. Brinkley, D. F. Dolan, Richard A. Altschuler, Joseph E. Hawkins, John F. Bateman

    Published 1990
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  15. 15
    Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects

    Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects by William R. Wilcox

    Published 2003
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  16. 16
    Connective tissue anomalies in patients with spontaneous cervical artery dissection

    Connective tissue anomalies in patients with spontaneous cervical artery dissection by Alessia Giossi, Marco Ritelli, Paolo Costa, Andrea Morotti, Loris Poli, Elisabetta Del Zotto, Irene Volonghi, Nicola Chiarelli, Massimo Gamba, Paolo Bovi, Giampaolo Tomelleri, Monica Carletti, Nicoletta Checcarelli, Giorgio Meneghetti, M Morra, Mauro Chinaglia, Valeria De Giuli, Marina Colombi, Alessandro Padovani, Alessandro Pezzini

    Published 2014
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  17. 17
    Marfan's syndrome: early and severe form in siblings

    Marfan's syndrome: early and severe form in siblings by Maria de Fátima Leite, Nádia Barreto Tenório Aoun, Mônica Scott Borges, Maria Eliane Campos Magalhães, Luiz A. Christiani

    Published 2003
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  18. 18
    Ehlers-Danlos syndromes and Marfan syndrome

    Ehlers-Danlos syndromes and Marfan syndrome by Bert Callewaert, Fransiska Malfait, Bart Loeys, Anne De Paepe

    Published 2008
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  19. 19
    Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type

    Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type by Fransiska Malfait, Richard Wenstrup, Anne De Paepe

    Published 2010
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  20. 20
    Transparent Skin and Osteoporosis : A Study in Patients with Rheumatoid Disease

    Transparent Skin and Osteoporosis : A Study in Patients with Rheumatoid Disease by B McConkey, Gerald Fraser, A. S. Bligh

    Published 1965
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